Zobrazeno 1 - 10
of 16
pro vyhledávání: '"metabolism [Superoxide Dismutase]"'
Autor:
Moritz J. Frech, Katharina Huth, Jan Lukas, Maik Liedtke, Alexandra V Jürs, Andreas Hermann, Christin Völkner
Publikováno v:
International Journal of Molecular Sciences
Volume 21
Issue 20
International journal of molecular sciences 21(20), 7667-(2020). doi:10.3390/ijms21207667
International Journal of Molecular Sciences, Vol 21, Iss 7667, p 7667 (2020)
Volume 21
Issue 20
International journal of molecular sciences 21(20), 7667-(2020). doi:10.3390/ijms21207667
International Journal of Molecular Sciences, Vol 21, Iss 7667, p 7667 (2020)
Oxidative stress (OS) represents a state of an imbalanced amount of reactive oxygen species (ROS) and/or a hampered efficacy of the antioxidative defense system. Cells of the central nervous system are particularly sensitive to OS, as they have a mas
Autor:
Phillip C. Wong, Diana Wiesner, Francesco Roselli, Tobias M. Boeckers, Deniz Yilmazer-Hanke, Barbara Commisso, Linyun Tang, Albert C. Ludolph, Jochen H. Weishaupt, Najwa Ouali Alami, Luc Dupuis, David Bayer, Bernd Baumann, Thomas Wirth
Publikováno v:
Life science alliance 3(11), e201900571 (2020). doi:10.26508/lsa.201900571
Life Science Alliance
Life Science Alliance, Life Science Alliance LLC, 2020, 3 (11), pp.e201900571. ⟨10.26508/lsa.201900571⟩
Life Science Alliance, 2020, 3 (11), pp.e201900571. ⟨10.26508/lsa.201900571⟩
Life Science Alliance
Life Science Alliance, Life Science Alliance LLC, 2020, 3 (11), pp.e201900571. ⟨10.26508/lsa.201900571⟩
Life Science Alliance, 2020, 3 (11), pp.e201900571. ⟨10.26508/lsa.201900571⟩
Chemogenetic motoneuron excitation and astrocyte GPCR-Gi signaling restore blood–spinal cord barrier, disrupted in four ALS mouse models, revealing its role in disease progression but not initiation.
Blood–spinal cord barrier (BSCB) disrupti
Blood–spinal cord barrier (BSCB) disrupti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93218dfe1100975b7bc1fb24ea761df4
https://pub.dzne.de/record/164314
https://pub.dzne.de/record/164314
Publikováno v:
Free radical research 48(2), 239-250 (2013). doi:10.3109/10715762.2013.861598
Due to its high nitrogen content, melamine was deliberately added to raw milk for increasing the apparent protein content. Previous studies showed that melamine-induced apoptosis and oxidative damage on PC12 cells and rats' hippocampus. Several evide
Autor:
Aikaterini Nanou, Ke Ning, Pamela J. Shaw, Adrian Higginbottom, Matthew Wyles, Chiara F. Valori, Mimoun Azzouz
Publikováno v:
Molecular Therapy
Molecular therapy 21(8), 1486-1496 (2013). doi:10.1038/mt.2013.115
Molecular therapy 21(8), 1486-1496 (2013). doi:10.1038/mt.2013.115
Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disorder with no effective treatment to date. Despite its multi-factorial aetiology, oxidative stress is hypothesized to be one of the key pathogenic mechanisms. It is thus propos
Autor:
Giuseppina Maccarinelli, Daniela Uberti, Maurizio Memo, Mery Montinaro, Giulia Ferrari-Toninelli, Sara Anna Bonini
Publikováno v:
Life Sciences. 92:903-910
Aim Oxidative stress is considered one of the main events that lead to aging and neurodegeneration. Antioxidant treatments used to counteract oxidative damage have been associated with a wide variety of side effects or at the utmost to be ineffective
Autor:
Isil Keskin, Elin Forsgren, Jonathan D. Gilthorpe, Anna Birve, Dale J. Lange, Peter M. Andersen, Stefan L. Marklund, Matthis Synofzik, Markus Weber
Publikováno v:
PLOS ONE 11(2), e0150133 (2016). doi:10.1371/journal.pone.0150133
PLoS ONE, Vol 11, Iss 2, p e0150133 (2016)
PLoS ONE
PLoS ONE, Vol 11, Iss 2, p e0150133 (2016)
PLoS ONE
Mutations in superoxide dismutase-1 (SOD1) are a common known cause of amyotrophic lateral sclerosis (ALS). The neurotoxicity of mutant SOD1s is most likely caused by misfolded molecular species, but disease pathogenesis is still not understood. Prop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a04c3ab95ca3fc0c1f8e436bc49b5f91
https://pub.dzne.de/record/138409
https://pub.dzne.de/record/138409
Autor:
Vercruysse, Pauline, Sinniger, Jérôme, Dreyhaupt, Jens, Grehl, Torsten, Hermann, Andreas, Grosskreutz, Julian, Witting, Anke, Van Den Bosch, Ludo, Spreux-Varoquaux, Odile, Group, GERP ALS Study, Ludolph, Albert C, Dupuis, Luc, El Oussini, Hajer, Borisow, Nadja, Holm, Theresa, Maier, Andre, Meyer, Thomas, Budde, Paula, Gruhn, Kai, Bewersdorff, Malte, Heneka, Michael, Storch, Alexander, Scekic-Zahirovic, Jelena, Frank, Tobias, Göricke, Bettina, Weishaupt, Jochen, Eger, Katharina, Hanisch, Frank, Zierz, Stephan, Boeck, Anna-Lena, Dengler, Reinhard, Koerner, Sonja, Kollewe, Katja, Dieterlé, Stéphane, Petri, Susanne, Prell, Tino, Ringer, Thomas, Zinke, Jan, Anneser, Johanna, Borasio, Gian Domenico, Chahli, Christine, Winkler, Andrea S, Boentert, Matthias, Stubbe-Draeger, Bianca, Young, Peter, Bogdahn, Ulrich, Franz, Steffen, Haringer, Verena, Weidner, Norbert, Benecke, Reiner, Meister, Stefanie, Prudlo, Johannes, Wittstock, Matthias, Dorst, Johannes, Hendrich, Corinna, Sperfeld, Anne-Dorte, Weiland, Ulrike, Neidhardt, Sabine, Schrank, Berthold, Beck, Marcus, Kraft, Peter, Toyka, Klaus, Ulzheimer, Jochen, Wessig, Carsten, Kassubek, Jan, Fischer, Wilhelm
Publikováno v:
Brain 139(4), 1106-1122 (2016). doi:10.1093/brain/aww004
Brain-A Journal of Neurology
Brain-A Journal of Neurology, Oxford University Press (OUP), 2016, 139 (4), pp.1106-1122. ⟨10.1093/brain/aww004⟩
Brain-A Journal of Neurology, 2016, 139 (4), pp.1106-1122. ⟨10.1093/brain/aww004⟩
Brain-A Journal of Neurology
Brain-A Journal of Neurology, Oxford University Press (OUP), 2016, 139 (4), pp.1106-1122. ⟨10.1093/brain/aww004⟩
Brain-A Journal of Neurology, 2016, 139 (4), pp.1106-1122. ⟨10.1093/brain/aww004⟩
International audience; Amyotrophic lateral sclerosis, the most common adult-onset motor neuron disease, leads to death within 3 to 5 years after onset. Beyond progressive motor impairment, patients with amyotrophic lateral sclerosis suffer from majo
Autor:
Alessandro Viggiano, Bruno De Luca, Caterina Aurilio, Andrea Viggiano, Emanuela Viggiano, Davide Viggiano, M. Chiefari, Marcellino Monda
Publikováno v:
Brain Research. 1050:72-78
Three experiments were conducted in order to investigate the possible involvement of the reactive oxygen species in the nociception within the subnucleus caudalis of the spinal trigeminal nucleus (Vc). In the first experiment the extracellular level
Publikováno v:
Cellular and molecular life sciences 71(2), 287-297 (2013). doi:10.1007/s00018-013-1429-7
Cellular and molecular life sciences : CMLS
Cellular and molecular life sciences : CMLS
Despite indisputable progress in the molecular and genetic aspects of amyotrophic lateral sclerosis (ALS), a mechanistic comprehension of the neurodegenerative processes typical of this disorder is still missing and no effective cures to halt the pro
Autor:
Martin Kerschensteiner, Leanne Godinho, Petar Marinković, Thomas Misgeld, Monika S. Brill, Miriam S. Reuter
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America 109(11), 4296-4301 (2012). doi:10.1073/pnas.1200658109
Axonal transport deficits have been reported in many neurodegenerative conditions and are widely assumed to be an immediate causative step of axon and synapse loss. By imaging changes in axonal morphology and organelle transport over time in several